A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858665



Internal ID22042308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160291061..160291061hg38UCSC Ensembl
chr5:159718068..159718068hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256359
Supporting Variants
Samples
Known GenesCCNJL
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858665
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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